Hasil Pencarian - Radka Kremlíková Pourová

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  1. 1
    A TBC1D24 gene variant coincides with STRC compound heterozygosity in a family with hearing loss: a case report

    A TBC1D24 gene variant coincides with STRC compound heterozygosity in a family with hearing loss: a case report oleh Martin Schwarz, Kamila Hanková, Markéta Havlovicová, Radka Kremlíková Pourová, Jan Bouček

    Diterbitkan 2024-10-01
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  2. 2
    The Key Role of Purine Metabolism in the Folate-Dependent Phenotype of Autism Spectrum Disorders: An In Silico Analysis

    The Key Role of Purine Metabolism in the Folate-Dependent Phenotype of Autism Spectrum Disorders: An In Silico Analysis oleh Jan Geryk, Daniel Krsička, Markéta Vlčková, Markéta Havlovicová, Milan Macek, Radka Kremlíková Pourová

    Diterbitkan 2020-05-01
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  3. 3
    Speech Perception and Production in Cochlear Implant Recipients with Pendred Syndrome

    Speech Perception and Production in Cochlear Implant Recipients with Pendred Syndrome oleh Jiri Skrivan, Michal Jurovcik, Zdenka Aksenovova, Jaromír Astl, Radka Kremlikova Pourova, Petra Dytrych, Tomas Sieger

    Diterbitkan 2021-07-01
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  4. 4
    A boy with developmental delay and mosaic supernumerary inv dup(5)(p15.33p15.1) leading to distal 5p tetrasomy – case report and review of the literature

    A boy with developmental delay and mosaic supernumerary inv dup(5)(p15.33p15.1) leading to distal 5p tetrasomy – case report and review of the literature oleh Pavel Tesner, Jana Drabova, Miroslav Stolfa, Martin Kudr, Martin Kyncl, Veronika Moslerova, Drahuse Novotna, Radka Kremlikova Pourova, Eduard Kocarek, Tereza Rasplickova, Zdenek Sedlacek, Marketa Vlckova

    Diterbitkan 2018-05-01
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